CDC Hides Evidence of Link Between Vaccines and Autism

Thanks to a FOIA request for documents, the CDC has been caught deliberately altering data to try to cover up evidence linking mercury in vaccines with autism.
October 2, 2011

Deniers of the link between mercury-laden vaccines and autism are going to have a hard time denying the latest findings by the Coalition for Mercury-Free Drugs (CoMeD). The nonprofit group has obtained critical documents via a Freedom of Information Act (FOIA) request that exposes the US Center for Disease Control and Prevention’s (CDC) role in deliberately lying about and manipulating a key Danish study that showed a clear link between vaccines containing mercury and autism.In 2003, the journal Pediatrics published a study conducted in Denmark that observed a significant decline in autism rates following the country’s elimination of Thimerosal, a mercury-based component, from vaccines. But thanks to the CDC’s corrupting influence, the published version of the study in Pediatrics actually claimed the opposite, and alleged that removal of Thimerosal brought about an increase in autism rates. See here why the CDC’s published version of the study is bogus.

According to the documents, CDC officials removed large amounts of data from the study that showed a decline in autism rates following the removal of Thimerosal. The agency then twisted the remaining data to imply an increase in autism rates following the removal of Thimerosal, and suggested that there was no link between Thimerosal and autism.

Upon submission of the CDC’s tainted version of the study to Pediatrics, the study’s authors contacted CDC officials to let them know that the agency had incorrectly interpreted the data. They tried to tell the CDC that its figures and conclusions were wrong, and that corrections needed to be made. See here 14 studies commonly used to support the false assertion that vaccines DO NOT cause autism and other neurological conditions.

The CDC allegedly responded by saying that it would take a look at the incorrect data, but proceeded to submit the corrupted version of the study to Pediatrics anyway. After encouraging the editors of Pediatrics to perform an expedited review of the corrupted study, the CDC ended up convincing the journal to publish the fraudulent study, which it did in 2003.

Now that this critical information has been officially released for the world to see, CoMeD is pressing the CDC to conduct a full criminal investigation into the matter, and make a formal declaration about whether or not scientific fraud was involved. CoMeD is also calling for a full, immediate retraction of the corrupted study from Pediatrics.

“This should not be tolerated by those who are entrusted with our children’s health and well-being,” says Lisa Sykes, President of CoMeD.

H1N1 Vaccine caused 3,587 Miscarriages

That is a 700 percent increase in miscarriage incidence.

Recent data presented to the U.S. Centers for Disease Control and Prevention’s (CDC) Advisory Committee on Children’s Vaccines has revealed some shocking information about the effects of the H1N1 / swine flu vaccine on pregnant women. According to the report, the rate of miscarriage among pregnant women during the 2009 H1N1 / swine flu pandemic soared by over 700 percent compared to previous years, pointing directly to the vaccine as the culprit — but the CDC denies the truth and continues to insist nobody has been harmed.

According to the CDC, nearly 50 percent of all pregnant women were vaccinated with the H1N1 vaccine during the 2009 / 2010 influenza season. Those whose physicians instructed them to get a seasonal flu shot were three times more likely to get it, while those instructed specifically to get the H1N1 shot were ten times more likely to get it. And the numbers clearly show that along with the rise in vaccinations due to the H1N1 scare came the sharp increase in miscarriages, including a slew of actual reported adverse events.

But the CDC does not seem to care about the facts, as numerous reports indicate the agency has failed to report any of this vital information to vaccine suppliers. In fact, when presented with the data for the third time, Dr. Marie McCormick, chair of the U.S. Department of Health and Human Services (HHS) Vaccine Risk and Assessment Working Group, actually had the audacity to claim that there were no vaccine-related adverse events in pregnant women caused by the vaccine.

“This baseless and fallacious assessment by the CDC assessment group has given the green light to the CDC’s Advisory Committee on Immunization Practices (ACIP) to continue their recommendation to give the 2010/11 flu shot to all people, including pregnant women,” explained Eileen Dannemann, director of the National Coalition of Organized Women, presenter of the information.

“This upcoming 2010/11 flu vaccine contains the same elements that are implicated in the killing of these fetuses, the H1N1 viral component and the neurotoxin mercury (Thimerosal). Additionally, it contains two other viral strains — a three-in-one shot for all people.”

Overall, the number of vaccine-related “fetal demise” reports increased by 2,440 percent in 2009 compared to previous years, which is even more shocking than the miscarriage statistic. Meanwhile, the CDC continues to lie to the public about the vaccine, urging everyone, including pregnant women, to get it.

To read the report for yourself, visit: http://www.progressiveconvergence.c…

IDflu: Sanofi-Pasteur’s Vaccine Cocktail

by Luis R. Miranda
The Real Agenda
September 7, 2010

As The Real Agenda reported a few weeks ago, the globalists who created the fraudulent H1N1 influenza pandemic, widely recorded as such, are back hungrier than ever for more fraud and more dollars. Recently, the newspaper La Nacion of Costa Rica published an article concerning the availability of the new vaccine from the pharmaceutical company Sanofi-Pasteur called IDFlu. The article, like almost everything this newspaper publishes is full of lies and half truths, so I was forced to write an article that talks about the details that Irene Rodriguez, the newspaper’s writer, omitted.

This is the tiny needle used to inject IDflu which is sold as one of the new "conveniences" because the pinch people feel is not so painful.

I wrote her an e-mail describing the details that were omitted, although I do not expect her to re-write it with the information documented in the e-mail. “I read your article on the new vaccine from Sanofi- Pasteur called IDFlu. I am concerned about omission of important details about the vaccine.” These details are precisely those that are never described to the public and for which many people still believe it’s a great idea to get vaccinated continuously.

First, the vaccine is the first of several types that will be offered to the public as a “cocktail” with various viruses including the infamous H1N1. With this, the consumer no longer has the option to choose which vaccine he wants to use, but will have to take them all; all in one. This eliminates the right to choose. In fact, the vaccine contains three viruses:
A / New Caledonia/20/99 (H1N1) like strain (A / New Caledonia/20/99 (IVR-116)) 9 micrograms HA, A/Wisconsin/67/2005 (H3N2 ) like strain (A/Wisconsin/67/2005 (NYMC X-161), 9 micrograms HA, B / Malaysia/2506/2004 like strain (B/Malaysia/2506/2004) 9 micrograms HA. View the original document descriptive of the vaccine.Page 32

Second, the article does not highlight the list of side effects, which are as severe as in other types of vaccines: Blood and lymphatic system disorders,encephalomyelitis (inflammation of the brain and spinal cord), Neuritis, Guillain Barre Syndrome, Inflammation of blood vessels, seizures, neurological diseases and immunogenicity, or the appearance of immunological reactions that usually end in partial or complete paralysis. Page 39

In addition, the article does not say that the clinical studies were conducted only from the time the vaccine is injected up to three weeks later, a period during which it is difficult to detect serious side effects, such as those cited above, (especially immunogenicity) because they usually occur after that period. The pharmaceutical company follow ups conveniently end at the end of six months, meaning that it does not carefully observes side effects that appear later. Therefore, Sanofi-Pasteur cannot say it can rule out serious side effects caused by the use of the vaccine, because monitoring is not done. However, Sanofi-Pasteur says that these effects are rare or nonexistent (Bottom of Page 4). Based on what does it make this observation? Not through scientific studies.

Third, according to the descriptive document that details the origin, manufacture and composition of the vaccine, clinical studies were conducted in European populations. In other words, any result obtained in these studies can not be used to prove the vaccine’s effectiveness or safety in other populations. How is it that the sale of a product that has not been studied to see its efficacy or risk of side effects in specific populations is allowed on the market? This question should be asked to your Department of Health.

Fourth, the results obtained regarding the safety of the vaccine for human use are based on animal studies (5.3 on page 6) and these studies, according to the pharmaceutical company, DO show immunogenicity.

Fifth, safety studies were not conducted after the vaccine was placed on the market and neither were incompatibility or clinical studies on the effects the vaccine may have on human motor skills, for example, to operating a vehicle equipment or machines, etc.

Finally, the vaccine contains formaldehyde, or formalin -in its liquid form-, a toxic ingredient used in vaccines and whose cumulative effect weakens the immune system, causes genetic alterations, metabolic acidosis, circulatory shock, respiratory failure and acute renal failure. Formalin is also a sensitizer, which means it can make you sensitive or allergic to many other things. It is corrosive if ingested, and is a possible carcinogen. In addition to the above, vaccines usually contain other ingredients such as thimerosal, squalene, adjuvants, sodium chloride, potassium chloride, disodium phosphate dihydrate and potassium dihydrogen phosphate.

However, the news about this vaccine are not its ingredients, but its behavior in the body. According to details contained in the official document, the vaccine is not injected into the muscle as traditionally done. Sanofi uses a new method, the intradermal. The exact dose of 0.1 ml is injected just under the skin, for more immediate action. Is it possible that the same speed with which such acts in the supposed task of immunization can be seen in the appearance of side effects? The pharmaceutical company Sanofi-Pasteur does not detail anything about it.

Perhaps the only positive side, specifically for Costa Ricans, is that health authorities are not going to buy the vaccine from the pharmaceutical company, at least for now, so those who want to inject the cocktail of viruses and formalin will have to take 24 dollars out of their pockets to buy it from local pharmacies. In this case, there is no taxpayer money for enriching the bank accounts of the corporation Sanofi-Pasteur.

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